classificationLevel 1

Classification

Under the IVD Regulation classification assigns each in-vitro diagnostic device to a risk class-A, B, C or D-based on its intended use, the importance

GET/api/v1/systems/reg_ivdr/nodes/classification

Manual TranscriptionPublic Domain (EUR-Lex)Source

Hierarchy Explorer

Hierarchy ExplorerChevron to expand - click title to open

annex_viiiAnnex VIII - Classification Rules

class_aClass A - Low Risk

class_bClass B - Moderate Risk

class_cClass C - High Risk

class_dClass D - Highest Risk

Cross-system equivalences0

No cross-system equivalences mapped for this node.

Report a data issue